Canonical Allele Identifier: PA645476275
Gene: GCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 265685
ClinVar RCV Id: RCV000255962 RCV001804993 RCV003236578 RCV003401220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004474.2:p.Met1Val